Medical Device Recalls
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1 to 10 of 120 Results
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Z-1806-2023 - ICD-VR VISIA MRI AF XT OUS DF4, Model Number DVFB2D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1808-2023 - ICD-VR VISIA MRI AF S US/OUS DF4, Model Number DVFC3D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1791-2023 - ICD-VR VISIA AF XT OUS IS1/DF1, Model Number DVAB2D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1792-2023 - ICD-VR VISIA AF XT OUS DF4, Model Number DDVAB2D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1793-2023 - ICD-VR VISIA AF S US/OUS IS1/DF1, Model Number DVAC3D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1794-2023 - ICD-VR VISIA AF S US/OUS DF4, Model Number DVAC3D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1817-2023 - ICD-VR DVME3D4 MIRRO MRI, Model Number DVME3D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1816-2023 - ICD-VR DVME3D1 MIRRO MRI, Model Number DVME3D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1815-2023 - ICD-VR DVMD3D4 PRIMO MRI, Model Number DVMD3D4; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-1814-2023 - ICD-VR DVMD3D1 PRIMO MRI, Model Number DVMD3D1; Implantable Cardioverter Defibrillators | 1 | 06/16/2023 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
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